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Clinical variability of chromosome 22q11.2 deletion syndrome
22q11.2 deletion syndrome (22q11.2 DS) is a disorder that has multiple symptoms and affects various organs and systems. Despite the great variability of clinical manifestations, common 22q11.2 DS includes congenital heart defect, immunodeficiency, characteristic facial features, palatal defects, dev...
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| Pubblicato in: | Cent Eur J Immunol |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Polish Society of Experimental and Clinical Immunology
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5820982/ https://ncbi.nlm.nih.gov/pubmed/29472823 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5114/ceji.2017.72818 |
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